Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonate | HCID 85257 | — |
| Reactant | HCID 23039690 | HCID 23039690 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 23039727 | HCID 23039727 | — |
Reaction Steps
6.93 g (25 mmoles) of 2-(2,4-dichlorophenyl)-2-ethoxy-pentan-1-ol are dissolved in 20 ml of pyridine and converted into the corresponding mesylate by adding 3.15 g (27.5 mmoles) of methanesulfochloride. The reaction takes place exothermically with the precipitation of pyridine hydrochloride. After a reaction time of 1 hour, water is added and the mixture is extracted with diethyl ether. The combined extracts are washed with half-saturated sodium chloride solution, dried over sodium sulfate, filtered and freed from solvent in vacuo. Yield 8.6 g. 100 MHz-1H-NMR (CDCl3): δ=4.7 ppm ##STR37## 3.2-3.6 ppm (q, 2H, --OCH2CH3); 2.8 ppm (s, 3H, --OSO2CH3); 1.8-2.5 ppm (m, 2H, --CH2CH2CH3); 1.3 ppm (t, 3H, --OCH2CH3); 0.7-1.3 ppm (m, 5H, --CH2CH2CH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04945100 |
|---|
| Source dataset | uspto-grants-1990_07 |
|---|
| ORD ID | ord-f3ccfdc3dc1a479195ad3d7b3525ae9b |
|---|
| Source note | uspto-grants-1990_07 |
|---|